Sodium Hydroxide → 5-Chlorotryptamine
Reaction equation
[H-].[H-].[H-].[H-].[Li+].[Al+3].[Al+3].[Cl-].[Cl-].[Cl-].[Cl:11][C:12]1[CH:13]=[C:14]2[C:18](=[CH:19][CH:20]=1)[NH:17][CH:16]=[C:15]2[C:21](=O)[C:22]([NH2:24])=O.[OH-].[Na+].[O-]S([O-])(=O)=O.[Na+].[Na+].CCOCC.Cl>C1COCC1.CCOCC>[Cl:11][C:12]1[CH:13]=[C:14]2[C:18]([NH:17][CH:16]=[C:15]2[CH2:21][CH2:22][NH2:24])=[CH:19][CH:20]=1Participants
Reactant 6
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 5 °C
Procedure
Cool to 5° C., a suspension of LiAlH4 (40.97 g) in THF (700 ml). Add a solution of AlCl3 (53.9 g, 0.40 mole) to THF (645 ml) over about 30 minutes while maintaining the temperature at about 5° C. and 10° C. Add (2-(5-chloro-1H-Indol-3-yl)-2-oxo-acetamide (20 g, 0.09 mole) in THF (900 ml) while maintaining the temperature at between 5° C. and 7.5° C. When the addition is complete warm to room temperature. Stir overnight and then cool to 7° C. and slowly add a solution of NaOH 50% (342 g, 4.28 mol). After stirring for about 1 hour, add anhydrous Na2SO4 (30 g) and filter the suspension on a celite bed. Evaporate the filtrate to dryness to give an oil. Combine the and Et2O (500 mL) and add a solution of Et2O/HCl 4.5N (15 mL) at room temperature to give a solid. Stir the suspension at room temperature for 1 hour, filter, and wash with 50 mL Et2O, dry under vacuum at 50° C. to give the hydrochloride of the title compound.
Workup
- temperaturewhile maintaining the temperature at about 5° C.
- custom10° C
- temperaturewhile maintaining the temperature at between 5° C. and 7.5° C
- additionWhen the addition
- temperatureis complete warm to room temperature
- temperaturecool to 7° C.
- stirringAfter stirring for about 1 hour
- filtrationfilter the suspension on a celite bed
- customEvaporate the filtrate to dryness
- customto give an oil
- customto give a solid
- stirringStir the suspension at room temperature for 1 hour
- filtrationfilter
- washwash with 50 mL Et2O
- customdry under vacuum at 50° C.
Sources & evidence
- ORD record
- ord-edbda80ea6ea43fb8e093623dce34e14
- Source dataset
- uspto-grants-2007_01
- Patent number
- US07157488B2
Reaction notes
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